| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:32820060-32820300 | Common:2; Rare:126 | ||||
| chr20:33401441-33401642 | Rare:95 | ||||
| chr20:33443660-33444110 | Common:4; Rare:246; Clinvar:8; Clinvar (benign):4 | ||||
| chr20:33489801-33490214 | Common:6; Rare:270 | ||||
| chr20:33666757-33667022 | Rare:115 | ||||
| chr20:33674275-33674537 | Common:2; Rare:161 | ||||
| chr20:33686292-33686731 | Common:3; Rare:138 | ||||
| chr20:33720150-33720600 | Common:8; Rare:197 | ||||
| chr20:33732037-33732464 | Common:6; Rare:227 | ||||
| chr20:33811067-33812321 | Common:6; Rare:360 | ||||
| chr20:33993054-33993411 | Common:1; Rare:150 | ||||
| chr20:33993532-33994149 | Common:6; Rare:362 | ||||
| chr20:34112206-34112509 | Common:1; Rare:171 | ||||
| chr20:34303279-34303512 | Common:4; Rare:189; Clinvar:6; Clinvar (benign):4 | ||||
| chr20:34363136-34363342 | Rare:111 |